Canonical Allele Identifier: CA379966215

Gene: WT1

Linked Data

• ClinVar Variation Id: 1999647
• ClinVar RCV Id: RCV002819753
• gnomAD v4: 11-32435180-G-A
• MyVariant Identifiers: chr11:g.32456726G>A (hg19) ; chr11:g.32435180G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.32435180G>A , CM000673.2:g.32435180G>A	GRCh38
NC_000011.9:g.32456726G>A , CM000673.1:g.32456726G>A	GRCh37
NC_000011.8:g.32413302G>A	NCBI36
NG_009272.1:g.5362C>T , LRG_525:g.5362C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332351.9:c.181C>T	ENSP00000331327.5:p.Arg61Trp
ENST00000379077.9:c.181C>T	ENSP00000368368.5:p.Arg61Trp
ENST00000448076.9:c.181C>T	ENSP00000413452.5:p.Arg61Trp
ENST00000452863.10:c.181C>T MANE Select	ENSP00000415516.5:p.Arg61Trp
ENST00000639563.3:c.181C>T	ENSP00000492269.3:p.Arg61Trp
ENST00000332351.7:c.166C>T	ENSP00000331327.3:p.Arg56Trp
ENST00000379077.7:c.166C>T	ENSP00000368368.3:p.Arg56Trp
ENST00000448076.7:c.166C>T	ENSP00000413452.3:p.Arg56Trp
ENST00000452863.7:c.166C>T	ENSP00000415516.3:p.Arg56Trp
NM_000378.4:c.166C>T	NP_000369.3:p.Arg56Trp
NM_024424.3:c.166C>T	NP_077742.2:p.Arg56Trp
NM_024426.4:c.166C>T	NP_077744.3:p.Arg56Trp
NM_000378.5:c.181C>T	NP_000369.4:p.Arg61Trp
NM_024424.4:c.181C>T	NP_077742.3:p.Arg61Trp
NM_024426.5:c.181C>T	NP_077744.4:p.Arg61Trp
NR_160306.1:n.360C>T
NM_000378.6:c.181C>T	NP_000369.4:p.Arg61Trp
NM_024424.5:c.181C>T	NP_077742.3:p.Arg61Trp
NM_024426.6:c.181C>T MANE Select	NP_077744.4:p.Arg61Trp